A Phase 3 Randomized Study Comparing Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) followed by Ciltacabtagene Autoleucel versus Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) followed by Autologous Stem Cell Transplant (ASCT) in Participants with Newly Diagnosed Multiple Myeloma who are Transplant Eligible - EMN2868284528MMY3005

European Myeloma Network Stichting0 个研究点目标入组 723 人开始时间: 2024年3月28日最近更新: 2024年7月22日

适应症

试验速览

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•18 years of age or older, Participants with documented NDMM according to IMWG diagnostic criteria, for whom high-dose therapy and ASCT are part of the intended initial treatment plan., Measurable disease, as assessed by central laboratory, at screening as defined by any of the following: 1) Serum monoclonal paraprotein (M-protein) level =1.0 g/dL or urine M-protein level =200 mg/24 hours; or 2) Light chain MM without measurable disease in serum or urine: serum Ig free-light chain (FLC) =10 mg/dL and abnormal serum Ig kappa lambda FLC ratio., ECOG performance status of grade 0 or 1, Clinical laboratory values within prespecified range as listed in 5.1.1, page 55 of the protocol.

•Prior treatment with CAR-T therapy directed at any target., Any prior BCMA target therapy., Any prior therapy for MM or smoldering myeloma other than a short course of corticosteroids, Received a strong cytochrome P450 (CYP)3A4 inducer within 5 halflives prior to randomization, Received or plans to receive any live, attenuated vaccine (except for COVID-19 vaccines) within 4 weeks prior to randomization., Known active, or prior history of central nervous system (CNS) involvement or clinical signs of meningeal involvement of MM, Stroke or seizure within 6 months of signing Informed Consent Form (ICF)

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